HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503146Generated: October 30, 2026
Sodium Cyanide → 3-(3-fluorophenyl)propanenitrile
https://huagongshe.com/reaction/1503146
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-(2-Bromoethyl)-3-fluorobenzene | HCID 573129 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3-fluorophenyl)propanenitrile | HCID 10261240 | 87% |
Reaction Steps
3-Fluorophenethyl bromide (23, 1.00 g, 12.3 mmol) was diluted in dry DMF (25 mL). Sodium cyanide (1.06 g, 61.6 mmol) was added in one portion, and the mixture was heated to 60° C. under argon for 16 h. The mixture was cooled and concentrated, and the residue was partitioned between EtOAc and H2O (50 mL each). The layers were separated, and the aqueous phase was extracted with EtOAc (2×20 mL). The organic layers were washed with H2O and sat. aq. NaCl (50 mL each), dried over anhydrous sodium sulfate, and concentrated. The resulting oil was purified by flash column chromatography (SiO2), eluting with a gradient of 5% EtOAc in hexanes to 30% EtOAc in hexanes to yield the desired product as a colorless oil (0.638 g, 87%). 1H-NMR (500 MHz; CDCl3): δ 7.31 (td, J=7.9, 6.0 Hz, 1 H), 7.03-6.93 (m, 3 H), 2.96 (t, J=7.4 Hz, 2 H), 2.63 (t, J=7.4 Hz, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212144B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-e888f39008f34601ba259c862562d6eb |
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| Source note | uspto-grants-2015_12 |
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